ID
35554
Description
Study ID: 101468/192 Clinical Study ID: 101468/192 Study Title:A 52 Week Open-Label Extension Study of the Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS) Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: ropinirole Trade Name: Modutab,ZIPEREVE,ZEPREVE,REPREVE,ADARTREL,REQUIP,Zygara; Zygara,ZIPEREVE,ZEPREVE,Requip Depot,REQUIP,REPREVE,Modutab,ADARTREL Study Indication : Restless Legs Syndrome The study consists of 16 visits which are devided in 3 study books: Book 1: Screening (+Baseline), Day 2, Week 1, Week 2 , Week 3 , Week 4, Week 5, Week 6, Week 7, Week 8 Book 2: Week 12, Week 24, Week 36, Week 48, Week 52, Follow-up Book 3: Early withdrawal and Follow-up Each follow-up Visit takes place 7 +/- 3 days after last dose This document contains the Previous Study Information form. It has to be filled in for screening.
Mots-clés
Versions (1)
- 08/03/2019 08/03/2019 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
8 mars 2019
DOI
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Licence
Creative Commons BY-NC 3.0
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Long-Term Safety of Ropinirole in Subjects Suffering from Restless Legs Syndrome (RLS), 101468/192
Previous Study Information
- StudyEvent: ODM
Description
Previous Study Information
Alias
- UMLS CUI-1
- C2603343
- UMLS CUI-2
- C1533716
- UMLS CUI-3
- C0205156
Description
Protocol Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0008971
- UMLS CUI [1,2]
- C0600091
Description
Centre Number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0600091
- UMLS CUI [1,2]
- C0019994
Description
Patient Number
Type de données
text
Alias
- UMLS CUI [1]
- C2348585
Similar models
Previous Study Information
- StudyEvent: ODM
C0019994 (UMLS CUI [1,2])
C1533716 (UMLS CUI-2)
C0205156 (UMLS CUI-3)
C0600091 (UMLS CUI [1,2])
C0019994 (UMLS CUI [1,2])